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Antibacterial mechanism of inosine against Alicyclobacillus acidoterrestris
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Abstract
Inosine could potentially become a novel antibacterial agent against
A. acidoterrestris
as low-dose of inosine can prevent
A. acidoterrestris
contamination. However, until now the antibacterial mechanism of inosine targeting
A. acidoterrestris
is still unknown. In this study, to unravel the mechanism of inosine against
A. acidoterrestris
puzzle, the effects of inosine on bacterial surface hydrophobicity, intracellular protein content, cell membrane damage extent and permeability of the
A. acidoterrestris
were investigated. The results showed that inosine can effectively inhibit the growth and reproduction of
A. acidoterrestris
by destroying the integrity of cell membrane and increasing its permeability, causing the leakage of intracellular nutrients. Furthermore, the interaction networks of inosine target proteins were analyzed. The interaction networks further revealed that damage of bacterial cell membrane might be relevant to inosine’s effect on bacterial DNA replication and cell energy metabolism through regulating nucleotide synthesis and metabolism and the activity of translation initiation factors. Finally, the antibacterial mechanism of inosine against
A. acidoterrestris
was proposed.
Title: Antibacterial mechanism of inosine against
Alicyclobacillus acidoterrestris
Description:
Abstract
Inosine could potentially become a novel antibacterial agent against
A.
acidoterrestris
as low-dose of inosine can prevent
A.
acidoterrestris
contamination.
However, until now the antibacterial mechanism of inosine targeting
A.
acidoterrestris
is still unknown.
In this study, to unravel the mechanism of inosine against
A.
acidoterrestris
puzzle, the effects of inosine on bacterial surface hydrophobicity, intracellular protein content, cell membrane damage extent and permeability of the
A.
acidoterrestris
were investigated.
The results showed that inosine can effectively inhibit the growth and reproduction of
A.
acidoterrestris
by destroying the integrity of cell membrane and increasing its permeability, causing the leakage of intracellular nutrients.
Furthermore, the interaction networks of inosine target proteins were analyzed.
The interaction networks further revealed that damage of bacterial cell membrane might be relevant to inosine’s effect on bacterial DNA replication and cell energy metabolism through regulating nucleotide synthesis and metabolism and the activity of translation initiation factors.
Finally, the antibacterial mechanism of inosine against
A.
acidoterrestris
was proposed.
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